US2008038263A1PendingUtilityA1

Methods using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione for treatment of mantle cell lymphomas

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Assignee: ZELDIS JEROME BPriority: Aug 3, 2006Filed: Aug 1, 2007Published: Feb 14, 2008
Est. expiryAug 3, 2026(~0.1 yrs left)· nominal 20-yr term from priority
A61P 37/02A61P 35/02A61P 35/00A61K 45/06A61K 9/0053A61K 31/573A61K 9/0019A61K 39/3955A61K 39/39558A61K 31/454A61K 39/395
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Claims

Abstract

Methods of treating, preventing or managing mantle cell lymphomas are disclosed. The methods encompass the administration of an immunomodulatory compound of the invention known as Revlimid® or lenalidomide. The invention further relates to methods of treatment using this compound with chemotherapy, radiation therapy, hormonal therapy, biological therapy or immunotherapy. Pharmaceutical compositions and single unit dosage forms suitable for use in the methods of the invention are also disclosed.

Claims

exact text as granted — not AI-modified
1 . A method of treating mantle cell lymphoma in a human, which comprises administering to a human in need thereof a therapeutically effective amount of 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione.  
   
   
       2 . The method of  claim 1 , wherein the mantle cell lymphoma is relapsed, refractory or resistant to conventional therapy.  
   
   
       3 . The method of  claim 1  or  2 , wherein the amount of 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione administered is from about 1 to about 50 mg per day.  
   
   
       4 . The method of  claim 3 , wherein the amount of 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione administered is about 10, 15, 20 or 25 mg per day.  
   
   
       5 . The method of  claim 4 , wherein the amount of 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione administered is about 25 mg per day.  
   
   
       6 . The method of  claim 3 , wherein 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione administered is enantiomerically pure.  
   
   
       7 . The method of  claim 6 , wherein 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione administered is S enantiomer.  
   
   
       8 . The method of  claim 6 , wherein 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione administered is R enantiomer.  
   
   
       9 . The method of  claim 3 , wherein 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione is administered orally.  
   
   
       10 . The method of  claim 9 , wherein 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione is administered in the form of a capsule or tablet.  
   
   
       11 . The method of  claim 3 , wherein 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione is administered for 21 days followed by seven days rest in a 28 day cycle.  
   
   
       12 . The method of  claim 11 , wherein 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione is administered in an amount of about 25 mg per day for 21 days followed by seven days rest in a 28 day cycle.  
   
   
       13 . The method of  claim 12 , further comprising administration of rituximab in an amount of 375 mg/m 2  by intravenous infusion weekly.  
   
   
       14 . A method of treating mantle cell lymphoma, which comprises administering to a patient in need thereof a therapeutically effective amount of 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione and a therapeutically effective amount of a second active agent.  
   
   
       15 . The method of  claim 14 , wherein the second active agent is antibody, hematopoietic growth factor, cytokine, anti-cancer agent, antibiotic, cox-2 inhibitor, immunomodulatory agent, immunosuppressive agent, corticosteroid, or a pharmacologically active mutant or derivative thereof.  
   
   
       16 . The method of  claim 14 , wherein the second active agent is rituximab.

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